Phase 2 Lymphoma Trial, Recruiting NCT06566586 Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06566586
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are willing to take part voluntarily and agree to follow the study requirements by signing a consent form
  • People aged between 18 and 75 years old at the time of signing the consent form
  • People with a general health and activity level rated as reasonably functional (scored 0–2 on a standard oncology scale), and who are expected to live for more than 3 months
  • People who have been confirmed through a tissue biopsy to have one of the following types of B-cell lymphoma, diagnosed using 2022 World Health Organization criteria: a slow-growing (indolent) B-cell lymphoma that has come back or stopped responding to treatment, or Diffuse Large B-Cell Lymphoma (DLBCL)
  • People with relapsed or treatment-resistant slow-growing B-cell lymphoma who have already received at least one previous course of standard treatment
  • People who have at least one area of lymphoma that can be measured on scans
  • People whose major organs (such as heart, liver, and kidneys) are functioning adequately
  • Women of childbearing age who agree to use contraception during the study and for 6 months after it ends, have a negative pregnancy test within 7 days before joining, and are not breastfeeding; men who agree to use contraception during the study and for 6 months after it ends

Who may not be able to join:

  • People who have had, or currently have, another type of cancer within the past 3 years
  • People with known or suspected spread of lymphoma to the brain or spinal cord (central nervous system)
  • People with relapsed or treatment-resistant slow-growing B-cell lymphoma who have previously received a stem cell transplant using a donor's cells, or who received their own stem cell transplant within the 3 months before starting treatment
  • People with relapsed or treatment-resistant slow-growing B-cell lymphoma who still have significant side effects from previous treatments (above a mild level), not including hair loss or fatigue
  • People who have difficulty absorbing oral (swallowed) medications, such as those who cannot swallow, have ongoing diarrhoea, or have a bowel blockage
  • People who have had major surgery or a serious injury within 28 days before the study treatment starts
  • People who have experienced a serious blood clot or related event within 6 months before starting treatment
  • People with a history of substance abuse involving mind-altering drugs that has not been resolved, or people with a diagnosed mental health disorder
  • People with any serious or uncontrolled medical condition
  • People who have received a live vaccine or mRNA vaccine within 4 weeks before the first dose, or who plan to receive one during the study
  • People who have taken part in another cancer drug clinical trial within 4 weeks before the first dose
  • People who, in the opinion of the study doctor, have other conditions that could put them at risk or make it difficult to complete the study

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 8 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 13642138692

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Registry
ClinicalTrials.gov
Start date
6 November 2024
Est. completion
1 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall response rate (ORR); Complete response rate (CRR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov